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Research Article Free access | 10.1172/JCI107677
Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts 02114
Department of Anatomy, Harvard Medical School, Boston, Massachusetts 02115
Department of Physiology, Harvard Medical School, Boston, Massachusetts 02115
Find articles by DiBona, D. in: JCI | PubMed | Google Scholar
Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts 02114
Department of Anatomy, Harvard Medical School, Boston, Massachusetts 02115
Department of Physiology, Harvard Medical School, Boston, Massachusetts 02115
Find articles by Chen, L. in: JCI | PubMed | Google Scholar
Department of Medicine, Massachusetts General Hospital, Boston, Massachusetts 02114
Department of Anatomy, Harvard Medical School, Boston, Massachusetts 02115
Department of Physiology, Harvard Medical School, Boston, Massachusetts 02115
Find articles by Sharp, G. in: JCI | PubMed | Google Scholar
Published May 1, 1974 - More info
The effects of acute volume expansion and of intraluminal administration of cholera toxin have been examined in rabbit jejunum.
Acute volume expansion was shown to reverse the normal reabsorptive flux of water and cause significant fluid secretion. Phase and electronmicroscopic examination of the jejunal epithelium showed that marked distension of the intercellular spaces had occurred. Examination of the jejunal epithelium after treatment with cholera toxin showed that, in association with high rates of fluid secretion, the intercellular spaces were extremely small and lateral membranes of adjacent cells were in close apposition to one another. Thus the mechanisms of fluid secretion in these two situations would appear to be quite different. The secretion associated with volume expansion, and accompanied by a rise in venous pressure and bullous deformations of terminal junctions, could well be due to hydrostatic pressure applied through intercellular channels. The secretion of cholera appears to be unrelated to hydrostatic pressure and is more likely due to body-to-lumen active ion transport.
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